Method of preparing nitrocycloalkanone

ABSTRACT

METHOD OF PREPARING A NITROCYCLOALKANONE OF THE FORMULA   R&lt;(-CO-CH(-NO2)-)   WHERE R IS POLYMETHYLENE OR SUBSTITUTED POLYMETHYLENE COMPRISING CONTACTING A CYCLOALKENE WITH DINITROGEN TETROXIDE AND OXYGEN TO FORM A PEROXY NITRATE COMPOUND SUBSEQUENTLY CONTACTING SAID PEROXY NITRATE COMPOUND WITH A DENITRATING AGENT.

United States Patent Cifice 3,657,349 METHOD OF PREPARING NITROCYCLO- ALKANONE Donald R. Lachowicz, Todd S. Simmons, and Kenneth L. Kreuz, Fishkill, N.Y., assignors to Texaco Inc., New York, N.Y. No Drawing. Application Mar. 10, 1966, Ser. No. 541,431, now Patent No. 3,466,326, which is a continuation-inpart of application Ser. No. 466,816, June 24, 1965, now Patent No. 3,415,856. Divided and this application Feb. 19, 1969, Ser. No. 831,794

Int. Cl. C07c 45/00 US. Cl. 260-586 R 3 Claims ABSTRACT OF THE DISCLOSURE Method of preparing a nitrocycloalkanone of the formula:

where R is polymethylene or substituted polymethylene comprising contacting a cycloalkene with dinitrogen tetroxide and oxygen to form a peroxy nitrate compound subsequently contacting said peroxy nitrate compound with a denitrating agent.

This application is a division of application Ser. No. 541,431, filed Mar. 10, 1966 and now Pat. No. 3,466,326, which in turn is a continuation-in-part of Ser. No. 466,816 filed June 24, 1965 and now Pat. No. 3,415,856.

This invention relates to a combination method for the production of alkanedioic acids from cycloalkene. Further, it pertains to subcornbination methods of converting cycloalkene into the corresponding nitroperoxy (nitrocycloalkylperoxy nitrate) and nitrocycloalkanone compounds. The invention is still further directed to the nitroperoxy products as novel compounds formed as recoverable intermediates in the combination process of the invention.

Parent application, Ser. No. 466,816 now US. Pat. No. 3,415,856, represents our discovery of a method of pro ducing alkanoic and alkanedioic acids respectively from aliphatic alkenes and alkenoic acids together with their corresponding nitroperoxy and. nitroalkanone intermediates by reacting an aliphatic olefin with a mixture of dinitrogen tetroxide and oxygen to form the nitroperoxy intermediate with the subsequent treatment of the nitroperoxy intermediate with particular denitrating compounds to form the nitroalkanone intermediate which in turn can be hydrolyzed in the presence of an acid catalyst to form alkanoic and alkanedioic acids.

We have discovered, and this constitutes our invention, that broadly the method set forth in our parent application, Ser. No. 466,816 now US. Pat. No. 3,415,856, is suitable for converting cycloalkenes into nitrocycloalkylperoxy nitrates, nitrocycloalkanones and alkanedioic acids. More specifically the overall method and submethods of the invention are defined as follows:

3,657,349 Patented Apr. 18, 1972 FIRST STAGE The first stage of the overall method of the invention comprises simultaneously contacting a cycloalkene of the general formula:

(lg-DONG: R--CH-NO1 where R is as heretofore defined. Preferably R is polymethylene of from 3 to 5 carbons, most preferably 4.

The reaction temperature employed is advantageously between about 40 and 20 C. Higher reaction temperatures tend to facilitate the decomposition of the peroxynitrate product and at temperatures below the prescribed range the dinitrogen tetroxide would not function due to its inability to dissociate into monomeric nitrogen dioxide.

The reactant mole ratio of cycloalkene to oxygen to dinitrogen tetroxide in the reaction is advantageously between about 12110.5 and 1:30:15. However, the critically important aspect of the reactant ratio is the maintenance of the mole ratio of oxygen to dinitrogen tetroxide of at least about 2:1 during the entire reactant contacting in the first stage. If the ratio of reactant oxygen to reactant dinitrogen tetroxide falls substantially below the 2:1 ratio during the reaction, a mixture of nitroalkyl nitrates and nitrites and dinitro compounds results rather than the desired nitrocycloalkylperoxy nitrate. Excess oxygen even in excess of the stated ranges does not deleteriously affect the reaction.

The reaction time is normally between about one-half and 10- hours although longer and shorter periods may be employed.

The formed nitroeycloalkyl-peroxy nitrate is recovered, if desired, by standard means, e.g., a fractional distillation such as stripping the volatiles from the reaction mixture below about 0 C. under reduced pressure.

It is to be noted that the nitrating agent, dinitrogen tetroxide, is actually, an equilibrium mixture of dinitrogen tetroxide and nitrogen dioxide with the equilibrium being driven essentially to dinitrogen tetroxide at 0 C. and essentially 100% nitrogen dioxide at C. the term dinitrogen tetroxide as used herein denotes the equilibrium mixture as well as the pure N 0 compound.

Under advantageous conditions, the dinitrogen tetroxide is normally introduced into the reaction system at a rate between about 0.002 and 0.02 gram/minute/gram cycloalkene. However, the actual rate depends in large measure upon the rate of heat removal from the reaction system.

The oxygen employed may be in the pure form or in the diluted form such as air or in admixture with inert gases such as nitrogen and argon. Under advantageous conditions, the oxygen is introduced into the reaction system at a rate between about 5 and 40 mls./minute/gram cycloalkene.

To promote contact of the reactants in the first stage the reaction is desirably carried out under conditions of agitation in the presence of an inert liquid diluent having boiling points between about 30 and 100 C. such as n-hexane, nhcptane, carbon tetrachloride and diethyl ether.

The contact of the nitrogen dioxide and oxygen with the cycloalkene is accomplished by standard means such as combining streams of oxygen and gaseous dinitrogen tetroxide. or by passing a stream of oxygen over or through liquid dinitrogen tetroxide at a temperature between about and 21 C. to form a mixture of dinitrogen tetroxide and oxygen which in turn is bubbled through or otherwise contacted with the cycloalkcne. Another means of introducing oxygen and dinitrogen tetroxide is the simultaneous introduction of separate streams of the dinitrogcn tetroxide and oxygen into the cycloalkene keeping in mind that the ratio of oxygen to dinitrogen tetroxide in the reaction zone should be maintained at at least about "I The formed peroxynitratc can be isolated from the SECOND STAGE la the second stage of the overall method the nitroeycloalkylperoxy nitrate formed in the first stage of the for mula:

t:tt-ooNo,

It (Ill-NO;

where R is as heretofore defined. is then contacted with a denitrating agent such as those selected from the group where R. R. R. R", R and R are alkyl of from i to S carbons and R R and R are hydrogen or alkyl of from I to carbons. The reactant contacting is conducted prefcrably with agitation, at a temperature between about 60 and 70 C. in a mole ratio of denitrating agent to peroxy compound of at least about l:l. preferably less than about :l. to form the nilro-alkanone of the formula:

where R is as heretofore defined. The reaction of the second stage is more or less instantaneous after addition of reactants. The particular mode of bringing the reactions together depends on many things such an molecttlar weight of reactants and reactivity of peroxy material. Normally. the contacting lu accomplished by slow addition of the more reactive peroxy intermediate to the denitrating agent for heat temperature control.

The nitrocycloalkanone intermediate product can be recovered by standard recovery processes. for example. via forming derivatives. filtration. extraction or fractional distillation and combinations thereof.

Normally. inert diluent is not employed in the second stage of the overall process of the in ention if one of the reactants is in liquid form. However, if both reactants are in the solid stage then to facilitate interaction inert liqt'tid diluent is employed. for example. inert liquid dilucnt having a boiling point between about 30 and C.. such as pentane. hexane, carbon tetrachloride and diethyl ether. Agitation of the reaction mixture is also a preferred condition.

Specific examples of the denitrating agents contemplated herein are dimethyl formamide, diethyl formamide. dimethyl acctamide, dimcthyl sulfoxide. diethyl sulfoxide. tetramethylurca, tetraethylurea and hexamethylenephosphoramide.

Specific examples of the nitrocycloalkanone products in the second stage of the overall process are Z-nitrocyclohexanone. 2-nitrocyclopentanone, Z-nitrocycloheptanone. 2-nitro-3-methyl cyclopentanone. Z-nitro-4-phenyl cyclohexanone 2-nitro-3-carboxytetramethylene cyclohcxane.

THIRD STAGE in the third stage of the overall method the nitrokctone of the formula:

where R is as heretofore defined. recovered from the second stage is contacted with water in the presence of an acid member selected from the group consisting of mineral acid. hydrocarbon sulfonic acid and haloacetic acid having a dissociation constant in excess of 10 at a temperature between about 0 and C.. advantageously in a mole ratio of nitrocycloalkanone to acid member of at least about l:l and up to 'l:l0 and higher. in a mole ratio of nitrocyeloalltanone to water of at least about I22 and up to 1:20 and higher to form a carboxylic acid of the general formula:

where R is as heretofore defined.

This third stage of the reaction is normally conducted for a period in the range of 15 minutes to several hours. However. the actual reaction time will be dependent in large measure on the particular acid strength of the acid member employed. Under preferred conditions. the reaction mixture is agitated in order to facilitate contact between the reactants. Further. if both the acid and the nitrocycloalkanone are of a solid nature in order to afford better reactant contact inert liquid diluent is advantageously employed. For example. inert liquid diluent having a boiling point between about 50 and 150 C., such as acetic acid.

The water contact in the third stage is normally accomplished by first forming the final nitroeycloalkanone acid reaction mixture and then contacting with an excess of water. e.g.. pouring said reaction mixture into a stoichiometric excess of water maintained at a temperature of about 0 C.

The carboxylic acid product is then recovered by standard means such as by filtration and/or extracting the formed carboxylic acid with ether followed by stripping off the extractant from the extract solution to leave the carboxylic acid as residue. Examples of the final carboxyllc acid products contemplated herein are adlplc acid. alatarle acid. plmelle acid. IZ-methyl pentaaedlolc acid. .1- taothyl ltexnnedlolc acid. .t-pheayl hexaaedlole acld and .l-earboxy tetramethylene hexanedlolc acid.

Specific examples of the acid catalyst contemplated in stage three are sulfuric acid. phosphoric acid, nitric acid, trichloroacetic acid. methane sulfonic acid and ethane sulfonic acid. The acids employed are advantageously of an acid strength in respect to aqueous dilution of at least about 70 wt. percent of the concentrated state.

The combination processes and subcombination processes (Stages I, II, III) of the invention may be further defined by the following equations utilizing cyclohexane, tetramethylurea and sulfuric acid as the example reactants:

OONO:

OONO:

III.

Example I This example illustrates the first stage of the overall method.

To a magnetically stirred flask maintained at 0 C. in an ice bath there was charged 3.8 mls. of cyclohexene and 60 mls. of carbon tetrachloride. Through the charged cyclohexene-carbon tetrachloride mixture there was bubbled a stream of a mixture of dinitrogen tetroxide and oxygen in a mole ratio of about 1:14 at a rate of 56.5 mls./minute, said stream formed by passing a stream of oxygen over dinitrogen tetroxide at a rate of 56.5 mls./ minute. This introduction lasted for a 6 hour period. A total of 2.4 mls. of dinitrogen tetroxide was added. At the end of the dinitrogen tetroxide-oxygen treating period, the carbon tetrachloride and excess nitrating agent was removed via vacuum at 0 C. under 18 mm. Hg. The residue was an almost colorless oil and was determined by infrared analysis to be 2-nitrocyclohexylperoxy nitrate.

Example II This example illustrates the second stage of the overall method, namely, the conversion of the peroxy nitrate compound of Example I into the corresponding nitrocyclohexanone.

To a magnetically stirred flask there was added 20 mls. of tetramethylurea. To the flask there was then added dropwise all of the peroxy nitrate product produced in Example I maintaining the temperature between about 20 and 25 C. by control of the addition rate and the use of an ice bath. The reaction solution turned yellow and was very exothermic during the addition. When addition was complete the formed nitroketone in the resultant reaction solution was isolated therefrom in purified form by first diluting the resultant solution with 50 mls. of ether followed by the addition of sodium bicarbonate to the ether solution until a visual (CO emission) reaction ceased to take place, i.e., until all the nitric acid by-product was destroyed. The nitroketone was then precipitated from the 5 neutralized ether solution as its orange morpholine salt in an amount of 5.5 grams by the addition of morpholine to said solution with stirring in an amount of 3.5 mls. The precipitated morpholine salt was separated from the ether solution and the nitroketone was regenerated from said salt by dissolving said salt with dilute aqueous hydrochloric acid and extracting the nitroketone with ether, evaporating off the ether to give 2.10 grams of a yellow oil product which was identified by infrared spectrum analysis as 2-nitrocyclohexanone.

Example III This example illustrates the third stage of the overall method of the invention, namely, the conversion of the nitrocycloalkanone product of Example II into the cor- 0 responding alkanedioic acid.

To 10 mls. of concentrated sulfuric acid at C. there was added 0.78 gram of Z-nitrocyclohexanone formed in Example II. The resultant acid solution was stirred /z hour at 20 C. and was then poured on ice and continuously extracted with ether for 5 hours. The ether was distilled from the ether extract solution leaving 0.23 gram of a white residue having a melting point of 140-146 C. The aqueous mixture was again continuously extracted with ether for 24 hours. The ether was distilled from the second ether extraction leaving a white residue having a melting point of 146-149 C. weighing 0.38 g. Infrared analysis and melting point determined the white residues to be adipic acid in a total yield of 75.9 wt. percent.

We claim:

1. A method of preparing a nitrocycloalkanone of the formula:

where R is as heretofore defined with dinitrogen tetroxide and oxygen at a temperature between about --40 and 20 C. while maintaining the ratio of said oxygen to dinitrogen tetroxide during said contacting at least about 2:1 to form a peroxy nitrate compound of the formula:

R CH N 02 where R is as heretofore defined,

(b) subsequently contacting said peroxy nitrate compound with a denitrating agent at a temperature between about 60 and 70 C. in a mole ratio of said denitrating agent to said peroxy nitrate compound of at least about 1:1, said denitrating agent selected from the group consisting of where R R R R R and R are alkyl of from 1 to 5 carbons and where R R and R are hydrogen 7 or alkyl of from 1 to 5 carbons.

2. A method in accordance with claim 1 wherein said References Cited I contacting in (a) is conducted utilizing a mole ratio of Griswold et Chem Abstracts, VOL 64, 9609e cycloalkene to oxygen to dinitrogen tetroxide of between (19 about1:1:0.5 and1:30:1.5. Zhuk et al.: Chem. Abstracts, vol. 59, p. 17529g 3. A method in accordance with claim 1 wherein said 5 (1961). nitroketone is 2-nitrocyclohexanone, said cycloalkene is cyclohexene, said peroxy nitrate is 2-nitrocycl0hexyl- LEON ZITVERf Pnmary Exammer peroxy nitrate, said denitrating agent is tetramethylurea N. MORGENSTERN, Assistant Examiner and wherein the cycloalkene-oxygen-dinitrogen tetroxide 10 CL contact in step (a) is conducted in the presence of carbon tetrachloride diluent. I 14 537 P, 610 R, 666 A 

